首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Nicotine-Induced Norepinephrine Release in Hypothalamic Paraventricular Nucleus and Amygdala Is Mediated by N-Methyl-D-aspartate Receptors and Nitric Oxide in the Nucleus Tractus Solitarius
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Nicotine-Induced Norepinephrine Release in Hypothalamic Paraventricular Nucleus and Amygdala Is Mediated by N-Methyl-D-aspartate Receptors and Nitric Oxide in the Nucleus Tractus Solitarius

机译:尼古丁诱导下丘脑室旁核和杏仁核中去甲肾上腺素的释放是由N-甲基-D-天门冬氨酸受体和一氧化氮在介导的孤立核中介导的。

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The noradrenergic projections from brainstem nucleus tractus solitarius(NTS)to hypothalamic paraventricular nucleus(PVN)and amygdala(AMYG)are involved in nicotine-related stress responses and drug craving.Previous studies demonstrated that i.v.nicotine-induced norepinephrine(NE)release in the PVN and AMYG depends on nicotinic cholinergic receptors in the brainstem.However,the direct site and mechanism of nicotine's action in brainstem are unknown.The present study determined the roles of NTS ionotropic glutamate receptors and nitric oxide(NO)in the effects of both local and systemic nicotine on NE release in PVN and AMYG.In male rats,an intra-NTS microinjection of nicotine(1.2 mu g free base)or i.v.nicotine infusion(0.065 or 0.09 mg/kg)significantly increased NE levels in PVN and AMYG microdialysates.Prior microinjection of the N-methyl-D-aspartate(NMDA)receptor antagonist,DL-2-amino-5-phosphonopentanoic acid(0.75 or 1.5 mu g),but not an alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor antagonist,dose dependently nearly abolished both PVN and AMYG NE responses to nicotine administered into NTS or systemically.NO involvement was assessed with intra-NTS microinjections of the nonselective nitric oxide synthase inhibitor,NG-nitro-L-arginine methyl ester hydrochloride(10-30 nmol),or the NO scavenger,2-(4-carboxyphenyl)-4,4,5,5-tetra-methylimidazoline-1-oxyl-3-oxide(0.1-0.2 nmol);both agents dose dependently inhibited i.v.nicotine-induced NE release.These results indicate that nicotine-induced NE release in PVN and AMYG is mediated entirely through the local effects of nicotine on NTS glutamate afferents and NMDA receptors that,in part,stimulate NO production,resulting in activation of noradrenergic neurons.Therefore,nicotine acts indirectly on noradrenergic NTS neurons to elicit NE release in forebrain structures.
机译:从大脑干索状核(NTS)到下丘脑室旁核(PVN)和杏仁核(AMYG)的去甲肾上腺素能投射都与尼古丁有关的应激反应和药物渴望有关。 PVN和AMYG依赖于脑干中的烟碱胆碱能受体,但尼古丁在脑干中作用的直接部位和作用机制尚不清楚。本研究确定了NTS离子型谷氨酸受体和一氧化氮(NO)在两种局部作用中的作用在雄性大鼠中,NTS内注射烟碱(1.2μg游离碱)或尼古丁输注(0.065或0.09 mg / kg)显着提高了PVN和AMYG微透析液中的NE水平。预先显微注射N-甲基-D-天冬氨酸(NMDA)受体拮抗剂DL-2-氨基-5-膦戊酸(0.75或1.5μg),但不注射α-氨基-3-羟基-5-甲基-4-异唑离子受体拮抗剂,剂量依赖性地几乎消除了对NTS或全身给药烟碱的PVN和AMYG NE的反应。非选择性一氧化氮合酶抑制剂NG-硝基-L-精氨酸甲酯盐酸盐在NTS内微量注射未评估其参与。 (10-30 nmol),或NO清除剂,2-(4-羧苯基)-4,4,5,5-四甲基咪唑啉-1-氧基-3-氧化物(0.1-0.2 nmol);两种药物的剂量均取决于剂量这些结果表明,烟碱诱导的PVN和AMYG中NE的释放完全是通过烟碱对NTS谷氨酸传入和NMDA受体的局部作用介导的,这些作用部分地刺激NO的产生,从而导致NO的激活。因此,尼古丁间接作用于去甲肾上腺素能神经元NTS神经元,以引起前脑结构中的NE释放。

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